# Megestrol Acetate

NDC: 0121-1038
Generic name: Megestrol Acetate
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20251017

FDA application: ANDA077404

## Active ingredients

- MEGESTROL ACETATE: 400 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-1038"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-1038
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d5b58cd-cbb1-4f5c-b13f-63185c0f8e31